Hederacoside C通过调控MAPK信号通路调节egf诱导的人气道上皮细胞MUC5AC粘蛋白基因表达

IF 3 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Biomolecules & Therapeutics Pub Date : 2025-05-01 Epub Date: 2025-04-30 DOI:10.4062/biomolther.2025.054
Rajib Hossain, Md Solayman Hossain, Hyun Jae Lee, Choong Jae Lee
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引用次数: 0

摘要

Hedera coside C是一种从Hedera helix中分离的活性化合物,已被用于治疗炎症性呼吸系统疾病,该研究旨在评估Hedera coside C在减轻表皮生长因子(EGF)诱导的气道MUC5AC粘蛋白基因表达方面的潜力。用hederacoside C预处理人肺黏液表皮样NCI-H292细胞30分钟,随后用EGF刺激24小时。研究还检测了hederacoside C对EGF诱导的丝裂原活化蛋白激酶(MAPK)信号通路的影响。结果表明,hederacoside C通过抑制EGF受体(EGFR)磷酸化、MAPK/细胞外信号调节激酶(ERK) 1/2 (MEK1/2)、p38 MAPK、ERK 1/2 (p44/42)磷酸化和特异性蛋白-1 (Sp1)的核表达,抑制MUC5AC粘蛋白mRNA表达和粘膜糖蛋白的产生。这些发现表明,hederacoside C可能通过抑制NCI-H292细胞中EGFR-MAPK-Sp1信号通路来降低egf诱导的粘蛋白基因表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hederacoside C Modulates EGF-Induced MUC5AC Mucin Gene Expression by Regulating the MAPK Signaling Pathway in Human Airway Epithelial Cells.

This study aimed to evaluate the potential of hederacoside C, an active compound isolated from Hedera helix, which has been used for managing inflammatory respiratory diseases, in attenuating epidermal growth factor (EGF)-induced airway MUC5AC mucin gene expression. Human pulmonary mucoepidermoid NCI-H292 cells were pretreated with hederacoside C for 30 min and subsequently stimulated with EGF for 24 h. The study also examined the effect of hederacoside C on the EGF-induced mitogen-activated protein kinase (MAPK) signaling pathway. The results showed that hederacoside C inhibited MUC5AC mucin mRNA expression and the production of mucous glycoproteins by suppressing the phosphorylation of the EGF receptor (EGFR), as well as the phosphorylation of MAPK/extracellular signal-regulated kinase (ERK) 1/2 (MEK1/2), p38 MAPK, ERK 1/2 (p44/42), and the nuclear expression of specificity protein-1 (Sp1). These findings suggest that hederacoside C has the potential to reduce EGF-induced mucin gene expression by inhibiting the EGFR-MAPK-Sp1 signaling pathway in NCI-H292 cells.

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来源期刊
CiteScore
6.60
自引率
8.10%
发文量
72
审稿时长
6-12 weeks
期刊介绍: Biomolecules & Therapeutics (Biomolecules & Therapeutics) (Print ISSN 1976-9148, Online ISSN 2005-4483) is an international, peer-reviewed, open access journal that covers pharmacological and toxicological fields related to bioactive molecules and therapeutics. It was launched in 1993 as "The Journal of Applied Pharmacology (ISSN 1225-6110)", and renamed "Biomolecules & Therapeutics" (Biomol Ther: abbreviated form) in 2008 (Volume 16, No. 1). It is published bimonthly in January, March, May, July, September and November. All manuscripts should be creative, informative, and contribute to the development of new drugs. Articles in the following categories are published: review articles and research articles.
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